Canonical Allele Identifier: CA2200883258
Gene: HBA1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000016.10:g.177320A= , CM000678.2:g.177320A= GRCh38
NC_000016.9:g.227319A= , CM000678.1:g.227319A= GRCh37
NC_000016.8:g.167319A= NCBI36
NG_000006.1:g.38183A=
NG_059186.1:g.5670A=

Transcript Alleles

HGVS Amino-acid change
ENST00000320868.9:c.338A= MANE Select ENSP00000322421.5:p.His113=
ENST00000397797.1:c.242A= ENSP00000380899.1:p.His81=
ENST00000472694.1:n.474A=
NM_000558.4:c.338A= NP_000549.1:p.His113=
NM_000558.5:c.338A= MANE Select NP_000549.1:p.His113=